FDA Inspection 837256 — Indilab, Inc.

Indilab, Inc. — FEI 1450962

The FDA completed an inspection of Indilab, Inc. on June 24, 2013 in Franklin Park, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 24, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Franklin Park, IL (United States)